WHR1

Inactive serine/threonine-protein kinase 19 · P49842 · WHR1 on Sugi Atlas →

4,625 patent compounds predicted against WHR1, 2,374 high-confidence (nearest known ligand ≥ 0.5)

Top predicted compounds (top 20 by supporting neighbours, then confidence)

CompoundConfidenceSupporting neighbours
SCHEMBL3779698 SCHEMBL3779698 0.67 7/20
Hydrochloric Acid Hydrochloric Acid (SCHEMBL3639996) 0.66 7/20
SCHEMBL2170933 SCHEMBL2170933 0.50 5/20
SCHEMBL10036161 SCHEMBL10036161 0.43 5/20
Trifluoroacetic Acid Trifluoroacetic Acid (SCHEMBL4965758) 0.52 4/20
SCHEMBL3318248 SCHEMBL3318248 0.52 4/20
SCHEMBL3319202 SCHEMBL3319202 0.51 4/20
SCHEMBL3319575 SCHEMBL3319575 0.51 4/20
Trifluoroacetic Acid Trifluoroacetic Acid (SCHEMBL4969262) 0.49 4/20
SCHEMBL4524523 SCHEMBL4524523 0.46 4/20
Trifluoroacetic Acid Trifluoroacetic Acid (SCHEMBL2831633) 0.36 4/20
SCHEMBL2914245 SCHEMBL2914245 0.58 3/20
SCHEMBL2923197 SCHEMBL2923197 0.53 3/20
SCHEMBL8076201 SCHEMBL8076201 0.52 3/20
SCHEMBL2170706 SCHEMBL2170706 0.51 3/20
SCHEMBL8070274 SCHEMBL8070274 0.50 3/20
SCHEMBL8070244 SCHEMBL8070244 0.49 3/20
SCHEMBL2170980 SCHEMBL2170980 0.48 3/20
SCHEMBL2170380 SCHEMBL2170380 0.47 3/20
SCHEMBL3635656 SCHEMBL3635656 0.47 3/20

Clinical trials — most relevant to WHR1 by text similarity (a relevance ranking, not an exhaustive list)

TrialPhaseStatus
Cisplatin to Patients With Pancreatic Cancer and Homologous Recombination Deficiency PHASE2/PHASE3RECRUITING
Safety, Tolerability and Efficacy for CGF166 in Patients With Unilateral or Bilateral Severe-to-profound Hearing Loss PHASE1/PHASE2COMPLETED
Satraplatin and Prednisone to Treat Prostate Cancer PHASE2COMPLETED
Alrizomadlin (APG-115) in Subjects With BAP1 Cancer Syndrome and Early-Stage Mesothelioma PHASE2WITHDRAWN
Efficacy and Safety Study of Niraparib in Melanoma With Genetic Homologous Recombination (HR) Mutation PHASE2UNKNOWN
Treatment Duration Increment and Pharmacodynamic Study of CX-4945 in Patients With Basal Cell Carcinoma (BCC) PHASE1COMPLETED
A Phase I Trial of SHR3162 in Subjects With Advanced Solid Tumors PHASE1COMPLETED
Bortezomib Followed by Pembrolizumab and Cisplatin in metTNBC EARLY_PHASE1RECRUITING
Prospective Validation of a DNA Damage Repair-Hippo Pathway Signature in Patients With Advanced Gastric Cancer nanUNKNOWN
Characterization of WAGR Syndrome and Other Chromosome 11 Gene Deletions nanCOMPLETED
Whole-genome Sequencing Study in Patients With Diminished Ovarian Reserve nanUNKNOWN
Gene Mutations and Rescue in Human Congenital Diaphragmatic Hernia nanUNKNOWN
A Proof of Concept Study for the DNA Repair Driven by the Mesenchymal Stem Cells in Critical COVID-19 Patients nanCOMPLETED
Diaphragmatic Hernia Research & Exploration, Advancing Molecular Science nanRECRUITING
Global Profiling of Gene and Protein Expression Associated With Coronary Heart Disease Reversal nanCOMPLETED
Molecular Studies on Hereditary Haemorrhagic Telangiectasia Families nanRECRUITING
Germline Alterations of Tumor Susceptibility Genes in New York Cancer Patients nanACTIVE_NOT_RECRUITING
Abnormalities in the Effects of Insulin and Exercise on Glucose- and Lipid Metabolism in Obesity and Type 2 Diabetes nanCOMPLETED
Genetic Analyses of Nonsyndromic and Syndromic Deafness in Pakistan nanENROLLING_BY_INVITATION
Genetic Basis of Non Syndromic Congenital Diaphragmatic Hernia nanCOMPLETED
Epidemiology of Pituitary Tumours: Prevalence of Associated Neoplasia nanUNKNOWN
Identification of Genetic Factors Implicated in Orofacial Cleft Using Whole Exome Sequencing nanRECRUITING
SMYD3-Driven Metabolic Rewiring in Colorectal Liver Metastases nanNOT_YET_RECRUITING
A Retrospective and Prospective Natural History Study of Patients With WHIM Syndrome nanWITHDRAWN
Genetic Study of Age-Related Macular Degeneration nanCOMPLETED
Identifying Genes and Mutations Underlying Retinitis Pigmentosa and Allied Diseases nanUNKNOWN
A Prospective Study of Molecular Detection of Salvageable Early Recurrent Nasopharyngeal Carcinoma After Radiotherapy nanCOMPLETED
Aberrant Splicings Due to Microsatellite Instability in Colorectal Cancer : Physiopathological and Clinical Impact nanUNKNOWN
Genetic Clues to Chordoma Etiology: A Protocol to Identify Sporadic Chordoma Patients for Studies of Cancer-Susceptibility Genes nanACTIVE_NOT_RECRUITING
Chordoma Family Study nanCOMPLETED

Related proteins — ESM-2 sequence neighbours (a WHR1 binder may also engage these)

ProteinNameSimilarity
Q9JHN8 1.000 Q9JHN8 →
A0A1L8F8I9 0.983 A0A1L8F8I9 →
Q6PGY6 0.977 Q6PGY6 →
Q9ESJ4 0.976 Q9ESJ4 →
Q96RY7 0.976 Q96RY7 →
Q14AI0 0.976 Q14AI0 →
Q8VZC9 0.976 Q8VZC9 →
CPSF1 Cleavage and polyadenylation specificity factor subunit 1 0.976 landscape →
Q10QS7 0.975 Q10QS7 →
A2CEI4 0.975 A2CEI4 →
Q9NZQ3 0.975 Q9NZQ3 →
Q8IV36 0.975 Q8IV36 →
A7E2V1 0.974 A7E2V1 →
Q08DK0 0.974 Q08DK0 →
A0AVI4 0.974 A0AVI4 →
Q9EPU4 0.974 Q9EPU4 →
Q8K304 0.974 Q8K304 →
A1A4I9 0.974 A1A4I9 →
B2GV24 0.974 B2GV24 →
Q7ZYP6 0.974 Q7ZYP6 →
Q38899 0.974 Q38899 →
UFL1 E3 UFM1-protein ligase 1 0.974 landscape →
NAT10 RNA cytidine acetyltransferase 0.973 landscape →
P0CI65 0.973 P0CI65 →
Q4QQS8 0.973 Q4QQS8 →
Q7TQK1 0.973 Q7TQK1 →
Q28DV7 0.973 Q28DV7 →
Q8CCJ3 0.973 Q8CCJ3 →
Q8R4H7 0.973 Q8R4H7 →
Q5ZL91 0.973 Q5ZL91 →